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Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss. (2023)

First Author: Lewis MA

Attributed to: GEroscience and Multi-Morbidity: identifying targets for intervention (GEMM) funded by SPF

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/2023.04.27.23289040

PubMed Identifier: 37163093

Publication URI: http://europepmc.org/abstract/MED/37163093

Type: Journal Article/Review

Parent Publication: medRxiv : the preprint server for health sciences